"Genome-Nilou Lab"[submitter] AND "LOC126860392"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95352	NM_006269.2(RP1):c.5008G>A (p.Ala1670Thr)	LOC126860392, RP1 (A1670T)	Single nucleotide variant (missense variant)	Retinal dystrophy +4 more	GBenign
Select item 95354	NM_006269.2(RP1):c.5071T>C (p.Ser1691Pro)	LOC126860392, RP1 (S1691P)	Single nucleotide variant (missense variant)	Retinal dystrophy +4 more	GBenign
Select item 95355	NM_006269.2(RP1):c.5175A>G (p.Gln1725=)	LOC126860392, RP1	Single nucleotide variant (synonymous variant)	Retinal dystrophy +4 more	GBenign

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